Home Cart Sign in  
Chemical Structure| 151746-34-8 Chemical Structure| 151746-34-8

Structure of 151746-34-8

Chemical Structure| 151746-34-8

*Storage: {[sel_prStorage]}

*Shipping: {[sel_prShipping]}

,{[proInfo.pro_purity]}

4.5 *For Research Use Only !

{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]} Purity: {[proInfo.pro_purity]}

Change View

Size Price VIP Price

US Stock

Global Stock

In Stock
{[ item.pr_size ]} Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price, item.vip_usd) ]}

US Stock: ship in 0-1 business day
Global Stock: ship in 5-7 days

  • {[ item.pr_size ]}

In Stock

- +

Please Login or Create an Account to: See VIP prices and availability

US Stock: ship in 0-1 business day
Global Stock: ship in 2 weeks

  • 1-2 Day Shipping
  • High Quality
  • Technical Support
Product Citations

Alternative Products

Product Details of [ 151746-34-8 ]

CAS No. :151746-34-8
Formula : C18H16N4
M.W : 288.35
SMILES Code : NC1=CC=C(N=C2C=CC(C=C2)=NC3=CC=C(N)C=C3)C=C1
MDL No. :N/A

Safety of [ 151746-34-8 ]

Application In Synthesis of [ 151746-34-8 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 151746-34-8 ]

[ 151746-34-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 53760-27-3 ]
  • [ 62-53-3 ]
  • [ 151746-34-8 ]
YieldReaction ConditionsOperation in experiment
Ca. 40% With hydrogenchloride; ammonium peroxydisulfate; sodium chloride; In water; at 5℃; for 1h; To synthesize AT3, aniline (1.48 g, 0.016 mol) and 4,-40 -diaminodiphenylamine sulfate (4.73 g, 0.016 mol) were dissolved in HCl aqueous solution (1.0 N, 150 mL) containing 15 g of NaCl. A solution of ammonium persulfate (3.6 g, 0.016 mol) in HCl aqueous solution (1.0 N, 25 mL) was added at a rate of approximately 60 drops min1 to the previously described solution maintained at operational temperature of 5 C using a dropping funnel. The reaction mixture was stirred for 1 h at 5 C. The resulting precipitate was collected through filtration, followed by washing with large amounts of HCl aqueous solution (1.0 N, 400 mL). Then, the filtrate was washed with NH4OH solution (1.0 N, 100 mL) and followed by washing with copious amount of distilled water. Thus, a blue powder was further dried in dynamic vacuum oven at an operational temperature of 50 C for 24 h. The crude product of AT3 was obtained as blue powder with a yield of ~40%
With hydrogenchloride; ammonium peroxydisulfate; sodium chloride; In water; at 5℃; for 1h; AT was prepared by following the procedure reported in elsewhere[4]. 75 g of NaCl was dissolved in aqueous HCl solution (1.0 M,800 mL). To this solution, 4,4?-diaminodiphenylamine sulfate (23.65 g,0.796 mol) and aniline (7.40 g, 0.796 mol) were added. To this final solution, HCl (1.0 M, 200 mL) containing ammonium persulfate(18.00 g, 0.789 mol) was added with the help of a dropping funnel at 5 C at the rate of 60 drops/min. The reaction mixture was allowed tostir for 1 h at 5 C. Once the stirring was finished, the reaction mixture was subjected to filtration to collect the precipitate. The obtained precipitate was washed with aqueous HCl solution (1.0 M, 400 mL) andthen precooled to 0 C. Finally, 10% NH4OH solution (100 mL) and alarge amount of distilled water were used to wash the solid product andthen dried in a vacuum oven at 5 C overnight. The aniline trimer (AT)was obtained as a red solid.
 

Historical Records